rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is a rare inherited immune disorder causing severe, early-life infections.
is an inherited JAK3-related immune disorder causing severe early-life infections.
is a fast-growing blood cancer affecting immature T cells.
is an aggressive childhood cancer of immature T cells, usually treatable.
is a rare immune disorder causing T-cell weakness and HPV skin lesions.
is a rare immune disorder where a missing thymus weakens T cells.
is a rare blood cancer involving abnormal T cells.
is a cancer of T cells in the lymphatic system.
is a rare, aggressive blood cancer affecting mature T cells.
is a rare aggressive B-cell lymphoma with few cancer cells.
is a rare inherited immune disorder causing life-threatening infections in infancy.
is an asthma type driven by type 2 airway inflammation.
is a type of asthma with low inflammation markers and varied triggers.
is a late-stage syphilis complication that damages nerves and affects walking.
is difficulty recognizing familiar objects by touch despite normal sensation.
is a rare epilepsy triggered by touch or tactile stimulation.
is a tapeworm infection of the intestines, often from undercooked meat.
is a rare inflammatory disorder causing swelling, low platelets, and organ problems.
is a rare inflammation of large arteries, affecting aorta and branches.
is an artery inflammation (vasculitis) that narrows the aorta and branches.
is a temporary heart muscle weakness from stress, mimicking heart attack.
is an aggressive subtype of thyroid cancer that often needs prompt treatment.
is a rare genetic disorder with tall height, learning challenges, kidney abnormalities.